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Effect of Roselle-based Drink on Blood Pressure and Skin

Not Applicable
Completed
Conditions
Other Skin and Subcutaneous Infections
Interventions
Dietary Supplement: Drink
Registration Number
NCT05084443
Lead Sponsor
Chung Shan Medical University
Brief Summary

This randomized, placebo-controlled, double-blind, and cross-over study was designed to check whether the roselle-based drink (2 bottles every day) can alter blood pressure and skin condition in elderly healthy subjects.

Detailed Description

The subjects were assigned into two groups (control group and test group), each group subject was requested to drink 2 bottles every day (100 mL/bottle, one in the morning and another in the evening), the rate of drinking is 75.42%. There are 39 subjects (25 females and 14 males) completely involved in the thirteen-month trial (cross-over). Blood samples were collected at the initial, 3rd, 6th, 7th, 10th, 13th months of the trial. Skin examinations were performed at the initial, 6th, 7th, 13th months.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
52
Inclusion Criteria
  • Healthy adults
  • Subjects should not be under any medication
  • Subject must be able to drink
Exclusion Criteria
  • Subjects with chronic renal, liver or cardiac disorders, Diabetes, hyperlipidemia.
  • Also pregnant women, chain smokers, high alcohol consumers should not be included.

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Arm && Interventions
GroupInterventionDescription
Placebo/ControlDrinkPlacebo drink-- Orally (200 ml/day)
Roselle Based drink (Test)DrinkRoselle-Based Drink--- Orally (200 ml/day)
Primary Outcome Measures
NameTimeMethod
Blood pressure by sphygmomanometer (mmHg)6 months

Both systolic and diastolic blood pressure were changed after Roselle drink

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Chung Shan Medical University

🇨🇳

Taichung city, Taichung, Taiwan

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